Skin Recovery Clinical Trial
Official title:
Safety Assessment, Instrumental and Perceived Efficacy 21 Days of Use at Home - Bepantol Derma Spray® Dermal and Gynecological Acceptability Assessment.
In this study, researchers want to learn more about the effect of dexpanthenol dermal spray
on skin recovery after a dermatological procedure (peeling) in the intimate area of women.
After the peeling, participants will return within 3 weeks for 4 visits to the study center
to investigate the skin conditions such redness, irritation, softness and possible side
effects. In addition, study participants will be asked about their general acceptance of
dexpanthenol dermal spray.
The primary objective is to evaluate the efficacy of the test product to aid skin recovery
after peeling in the female intima and inguinal region.
Secondary objectives comprise clinical efficacy with respect to skin hydration, softness,
vitality, appearance etc. and skin recovery, consumer judgement of product performance and
acceptability, and safety.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT03852563 -
A Study to Gain Information How Well Dexpanthenol Derma Cream Helps the Face Skin to Recover After Cosmetic Lasering
|
N/A | |
| Completed |
NCT03853538 -
A Study to Gain Information How Well Dexpanthenol Dermal Spray Helps the Face Skin to Recover After Cosmetic Lasering
|
Phase 4 | |
| Completed |
NCT03853525 -
A Study to Gain Information How Well Dexpanthenol Dermal Spray Helps the Skin to Recover After Laser Hair Removal in the Groin and Intimate Area
|
Phase 4 |